Search results for "Monomer"

showing 10 items of 857 documents

Effect of solute association on the apparent adsorption isotherm. A model of the separation of non-racemic mixtures of enantiomers in achiral chromat…

1996

This article discusses the effect of solute association on the apparent adsorption isotherm and on the chromatographic peak profile. The modelling performed has shown that dimerization of a solute in a chromatographic system gives rise to an apparent adsorption isotherm of the non-linear type. This results first of all in peak broadening. Tailing or a fronting can be observed depending on the relative retention of the monomer and the dimer. Secondly, the retention of the solute depends on the amount of sample because of the non-linear character of the adsorption isotherm. As a result, an excess of one of two analytes with absolutely identical adsorption properties i.e. optical isomers, can …

ChromatographyElutionDimerOrganic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryAnalytical Chemistrychemistry.chemical_compoundMonomerAdsorptionchemistrySorption isothermEnantiomerEquilibrium constantChromatographia
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Performance of a series of novel N-substituted acrylamides in capillary electrophoresis of DNA fragments

1996

DNA separations by capillary electrophoresis in viscous solutions of novel polymers, made with Ω-hydroxyl, N-substituted acrylamides (notably N-acryloyl amino propanol, AAP and N-acryloyl amino butanol, AAB) are evaluated. Whereas in standard poly(acrylamide), at 6% concentration, the theoretical plate number (N) does not exceed 500 000, in 6% poly(AAP) N reaches 922 000 and in 6% poly(AAB) N values as high as 1 200 000 are obtained. Also, copolymers of AAP and AAB give N values in excess of 1 million plates. The two novel monomers (AAP and AAB) remain extremely stable during alkaline hydrolysis and display very good hydrophilicity, while being devoid of the noxious habit of auto-polymeriza…

ChromatographyHydrogen bondButanolOrganic ChemistryGeneral MedicineAlkaline hydrolysis (body disposal)BiochemistryAnalytical ChemistryPropanolchemistry.chemical_compoundMonomerCapillary electrophoresischemistryAcrylamideAlkoxy groupJournal of Chromatography A
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Quantitative retention–structure and retention–activity relationships of barbiturates by micellar liquid chromatography

1998

Abstract Studies on the structural requirements of chromatographic surfaces to emulate in vitro the partitioning process in biomembranes are of great interest. The use of micellar mobile phases in RPLC modifies the hydrophobicity of the stationary phase and provides hydrophobic and electrostatic sites of interaction as a consequence of the adsorption of surfactant monomers to the chromatographic surface. Modified stationary phases in MLC could be structurally similar to biomembranes, but thorough studies are necessary to confirm this. In this paper we focus our attention on barbiturates. The influence of the nature and concentration of the surfactant (Brij 35, SDS and CTAB) and the mobile p…

ChromatographyOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundAdsorptionMonomerPulmonary surfactantchemistryStationary phaseMicellar liquid chromatographyPhase (matter)Journal of Chromatography A
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MALDI-TOF characterization of macromonomers

1996

Methacryloyl endfunctionalized oligostyrene macromonomers were characterized by matrix assisted laser desorption ionization/time of flight (MALDI-TOF) spectroscopy and by isocratic and gradient high performance liquid chromatography (HPLC). The molar mass distribution derived by the different techniques coincide for the investigated oligomers. Mixing experiments revealed that the MALDI-TOF peak areas do not necessarily represent the mixing ratio of the components. Combination of gradient HPLC and MALDI-TOF has resolved the chemical composition of the coupling products formed by reaction of the living anion with oxygen.

ChromatographyPolymers and PlasticsChemistryOrganic ChemistryMatrix isolationAnalytical chemistryMass spectrometryMacromonomerHigh-performance liquid chromatographyTime of flightMatrix-assisted laser desorption/ionizationMaterials ChemistryMolar mass distributionSpectroscopyMacromolecular Rapid Communications
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Preferential solvation of a dicyanate ester monomer and poly(sulfone) in different organic solvents by size-exclusion chromatography.

2002

Preferential solvation parameters A in the ternary systems solvent (1) -monomer (2) -polymer (3) were determined as a tool to measure the compatibility between the cyanate ester monomer Arocy B10 and poly(sulfone), PSF, in the presence of three organic solvents: tetrahydrofuran, dimethylformamide and dicloromethane. The A parameter was measured by size-exclusion chromatography at different monomer-to-polymer ratios. The quantitative evaluation was rigorously made at polymer-diluted conditions. PSF was found to be preferentially solvated by the monomer. Concerning the solvent used, systems containing tetrahydrofuran showed the strongest solvation, the lowest A values being those obtained in …

ChromatographyPolymersViscosityIntrinsic viscosityOrganic ChemistrySize-exclusion chromatographySolvationGeneral MedicineBiochemistryAnalytical ChemistrySolventGel permeation chromatographychemistry.chemical_compoundMonomerchemistrySolubilityPolymer chemistryChromatography GelSolventsDimethylformamideSulfonesTetrahydrofuranCyanatesJournal of chromatography. A
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Evaluation of molecular mass and tacticity of polyvinyl alcohol by non-equilibrium capillary electrophoresis of equilibrium mixtures of a polymer and…

2011

Non-equilibrium capillary electrophoresis of equilibrium mixtures (NECEEM) has been used to characterize polyvinyl alcohol (PVA). Commercial PVA samples with different molecular masses, from M(w)=15 up to 205 kDa, were used. According to the (13)C NMR spectra, the samples also differed in tacticity (stereoregularity). Mixtures of PVA and the anionic azo-dye Congo Red (CR) were injected in the presence of a borate buffer. The electropherograms gave a band and a peak due to the residual PVA-CR complex and the excess dye, respectively, plus a superimposed exponential decay due to the partial dissociation of the complex during migration. The stoichiometry of the PVA-CR complex, q=[monomer]/[dye…

Chromatographyintegumentary systemOrganic ChemistryElectrophoresis CapillaryCongo RedGeneral MedicineBiochemistryPolyvinyl alcoholDissociation (chemistry)Analytical ChemistryMolecular Weightchemistry.chemical_compoundElectrophoresisMonomerCapillary electrophoresischemistryStability constants of complexesPolyvinyl AlcoholTacticityBoratesSpectrophotometry UltravioletAzo CompoundsStoichiometryJournal of Chromatography A
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Molecular heterogeneity of the hemocyanin isolated from the king crabParalithodes camtschaticae

2000

Native Paralithodes camtschaticae hemocyanin is found as a mixture of dodecamers (24S; 80%) and hexamers (16S; 20%). Removal of Ca2+ ions by dialysis against EDTA-containing buffer solution at neutral pH induces complete dissociation of the 24S form into the 16S form. Under these conditions, a further increase in pH to 9.2 produces complete dissociation of the hexamers into monomers (5S). In both cases, the dissociation process is reversible. The dodecamer (24S) is composed of two different hexamers which can be discriminated only by ion-exchange chromatography in the presence of Ca2+ ions. At alkaline pH and in the presence of EDTA, two major monomeric fractions can be separated by ion-exc…

Chromatographymedicine.medical_treatmentHemocyaninBohr effectBuffer solutionBiochemistryDissociation (chemistry)Crystallographychemistry.chemical_compoundDodecameric proteinMonomerchemistrymedicineProtein quaternary structureOxygen bindingEuropean Journal of Biochemistry
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Characterization of gramicidin A in an inverted micellar environment. A combined high-performance liquid chromatographic and spectroscopic study

1992

We have investigated the conformational adaptability of gramicidin A incorporated into reverse micelles of sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/isooctane/water, a so far unexplored "host" membrane-mimetic model system for this peptide. A high-performance liquid chromatographic strategy previously developed for the study of gramicidin in phospholipid vesicles and normal micelles [Bañó et al. (1989) FEBS Lett. 250, 67; Bañó et al. (1991) Biochemistry 30, 886] has been successfully extended to this system. The method has permitted the separation of peptide conformational species, namely, double-stranded dimers and monomers, and an accurate quantitation of their proportion in the invert…

Circular dichroismChemical PhenomenaMacromolecular SubstancesProtein ConformationDimerMolecular Sequence DataSynthetic membraneFluorescence PolarizationPeptideBiochemistryMicelleDissociation (chemistry)chemistry.chemical_compoundAmino Acid SequenceChromatography High Pressure LiquidMicelleschemistry.chemical_classificationDioctyl Sulfosuccinic AcidChromatographyChemistry PhysicalCircular DichroismSpectrum AnalysisGramicidinSpectrometry FluorescenceMonomerchemistryGramicidinBiochemistry
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Confinement of chiral molecules in reverse micelles: FT-IR, polarimetric and VCD investigation on the state of dimethyl tartrate in sodium bis(2-ethy…

2008

Abstract The state of d and l -dimethyl tartrate confined within dry sodium bis(2-ethylhexyl) sulfosuccinate (AOT) reverse micelles dispersed in CCl 4 has been investigated by FT-IR spectroscopy, polarimetry, and vibrational circular dichroism (VCD). Measurements have been performed at 25 °C as a function of the solubilizate-to-surfactant molar ratio ( R ) at a fixed AOT concentration (0.158 M). The analysis of experimental data is consistent with the hypothesis that both enantiomers of dimethyl tartrate are mainly entrapped in the reverse micelles and located in proximity to the surfactant head-group region. The formation of this interesting self-organized chiral nanostructure involves som…

Circular dichroismInorganic chemistryInfrared spectroscopyTartrateMicellechemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPulmonary surfactantVibrational circular dichroismPhysical chemistryEnantiomerDimethyl tartrate Sodium bis(2-ethylhexyl) sulfosuccinate Reverse micelles Chiral nanostructures FT-IR spectroscopy Vibrational circular dichroism Optical rotationColloids and Surfaces A: Physicochemical and Engineering Aspects
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Dynamic Light Scattering Investigation of the Kinetics and Fidelity of Supramolecular Copolymerizations in Water

2017

The self-assembly of supramolecular copolymers facilitates the preparation of multifunctional materials, with tunable mechanical, electronic, or bioactive properties. Compared to covalent copolymerization protocols, controlling the molecular weight, stability, and monomer sequence of a multicomponent supramolecular copolymer remains limited. Here, we report a light scattering investigation of the charge-regulated supramolecular copolymerization in neutral buffer of physiological ionic strength, supported with electron microscopy and circular dichroism spectroscopy experiments. Dendritic anionic and cationic peptide comonomers self-assemble into AB-type heterocopolymers with a nanorod-like m…

Circular dichroismMaterials sciencePolymers and Plastics010405 organic chemistryOrganic Chemistrytechnology industry and agricultureSupramolecular chemistryCationic polymerizationmacromolecular substances010402 general chemistry01 natural sciencesLight scattering0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerDynamic light scatteringchemistryChemical engineeringIonic strengthPolymer chemistryMaterials ChemistryCopolymerMacromolecules
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